87863-08-9 Usage
Uses
Used in Organic Synthesis:
cis-3-Methylcyclobutanecarboxylic acid is utilized as a building block in organic synthesis for the creation of more complex molecules. Its unique structure and reactivity allow for the formation of various chemical compounds, contributing to the development of new materials and pharmaceuticals.
Used in Natural Products:
cis-3-Methylcyclobutanecarboxylic acid is found as a component in some natural products, where it contributes to their specific properties and functions. Its presence in these products highlights the compound's potential for use in the development of natural-based materials and substances.
Check Digit Verification of cas no
The CAS Registry Mumber 87863-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,6 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87863-08:
(7*8)+(6*7)+(5*8)+(4*6)+(3*3)+(2*0)+(1*8)=179
179 % 10 = 9
So 87863-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-4-2-5(3-4)6(7)8/h4-5H,2-3H2,1H3,(H,7,8)/t4-,5+
87863-08-9Relevant academic research and scientific papers
Compounds and Uses Thereof - 848
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Page/Page column 70, (2009/01/24)
This invention relates to novel compounds having the structural formula I below: and their pharmaceutically acceptable salts, tautomers or in vivo-hydrolysable precursors, compositions and methods of use thereof, wherein R1, R2, Rsu
Synthesis of Stereoisomeric 3-Substituted Cyclobutanecarboxylic Acid Derivatives
Dehmlow, Eckehard V.,Schmidt, Stefan
, p. 411 - 414 (2007/10/02)
The preparation of 3-substituted cyclobutanecarboxylic acids by ring forming malonic ester cycloalkylation/saponification/decarboxylation leads to 50:50 cis/trans mixtures.Only some polar ester derivatives 2 can be separated by chromatographic methods.Catalytic hydrogenation of 3-substituted cyclobutanecarboxylic acids 3, however, gives the cis acids 4 with 90-95 percent selectivity.Reduction of the same acids 3 by Zn in aqueous HCl/THF leads to the trans acids 6 with 90-93 percent selectivity.
